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Sugar-Amide Surfactant Micelles as Effective Reaction Fields for Enantioselective Hydrolysis of α-Amino Acid Esters

✍ Scribed by Kida, Toshiyuki; Kajihara, Keisuke; Isogawa, Kazuhiko; Zhang, Wanbin; Nakatsuji, Yohji; Ikeda, Isao; Akashi, Mitsuru

Book ID: 126155138
Publisher: American Chemical Society
Year: 2004
Tongue: English
Weight: 88 KB
Volume: 20
Category: Article
ISSN: 0743-7463
DOI: 10.1021/la0489662

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📜 SIMILAR VOLUMES

Enantioselective hydrolysis of an α-amin

Enantioselective hydrolysis of an α-amino acid ester in sugar-derived surfactant micelles

✍ Toshiyuki Kida; Kazuhiko Isogawa; Wanbin Zhang; Yohji Nakatsuji; Isao Ikeda 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 278 KB

## Nitrophenyl ester of Pphenylalanine hydrogen bromide was hydrolyzed much faster than that of the corresponding L-isomer in the micelles formed with sugarderived surfactants such as N-dodecyhnaltobionamide.